FDA UDI In Commercial Distribution 🇺🇸 United States

RENOVATION Knee Extraction

DI: 07611996121476 · Model: 75100801 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RENOVATION Knee Extraction
Primary DI
07611996121476
Version / Model
75100801
Catalog Number
75100801
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-25
Public Version
4
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
0aee895d-5229-4ccf-987f-66da63854d3e

Device Description

SAW-BLADE STRYKER S6 14.0X23.0X0.4MM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GFA BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 07611996121476

Customer Contacts